A set of ~800 largely isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Designed to fill gaps in deletion coverage and breakpoint placement; also used to replace older available deficiencies that have not been molecularly mapped.
Inferred to overlap with: Df(3R)ED6090.
The breakpoints of Df(3R)BSC804 predicted from the Release 5 genomic coordinates of the progenitor PBac{RB}Cchle01195 and P{XP}d09130 insertion sites are 3R:17851727 ;17959518 and the cytological breakpoints predicted from these coordinates are 94A1;94A2.